Category: Uncategorized

Tories propose nudge, big business AI initiative and ‘personal responsibility’ in place of adequate health care funding

Health spending by govt

A breakdown of spending on health care under each government up to 2016. Under the Major government, we saw a post code lottery of health care provision and patients were left for hours on end in hospital corridors. It’s a grim consideration that the Major government spent rather more on health care than the Conservatives in office since 2010.

Earlier this year, the prime minister was warned that patients being treated within the National Health Service are dying prematurely in hospital corridors, in a letter from A&E chiefs outlining “very serious concerns” about patient safety. 

Sixty-eight senior doctors in charge of some of the busiest accident and emergency departments in England and Wales said safety compromises are becoming “intolerable”. 

The letter includes accounts from frontline A&E doctors, one of whom warned 120 patients a day were being treated in corridors because of a lack of space on wards.

The letter said: “The fact remains that the NHS is severely and chronically underfunded. We have insufficient hospital and community beds and staff of all disciplines especially at the front door to cope with our ageing population’s health needs.”

Other issues raised in the letter, first reported in the Health Service Journal, include patients waiting up to 12 hours for a bed after doctors had decided to admit them, with queues of 50 patients waiting in one emergency department. May said that the cancellation of 55,000 appointments  was “part of the plan” for the NHS last winter, but said of her government’s response “nothing is perfect”.

The National Health Service (NHS) faces significant financial problems in many different areas. It is succeeding in treating more patients than in the past, but this rise in public need for health care, and rising costs coupled with very tight budgets, are translating into widespread pressures on the capacity of staff and managers to keep up with past performance and the standards the service sets itself.” 

Lengthening queues for treatment are happening despite the NHS treating more patients. In England, Scotland, Wales and Northern Ireland, the number of episodes of care provided in NHS hospitals has been rising. In England, for example, the number of episodes of care overseen by a hospital consultant has risen 11.4% between 2010/11 and 2015/16. It is just that the rise in the treatment provided is not keeping pace with the even faster rise in the number of people coming forward.

At the same time, EnglandScotland and Wales have all started in different ways to look at reducing the provision of treatments that may be deemed of ‘less benefit’ to patients. That means that some people who would have had treatment on the NHS before may not in future. 

This decade health services have seen some of the lowest spending increases in their history. In England, real annual increases are only around 1% a year.

Real terms spending has also been roughly flat per person since 2010 in WalesScotland and Northern Ireland.

This compares to an average increase of nearly 4% over the history of the NHS reflecting the fact that, as the OBR has found, an aging population, new technology and rising wealth all tend to increase health spending in a country.

Matt Hancock, the demedicalisation of illness and the neoliberal psychosocial model

Matt Hancock, the Secretary of State for Health and Social Care, has called on patients to have greater responsibility for their own health in the launch of new a policy paper entitled Prevention is better than cure which outlines a vision for a “new 21st-century focus on prevention”.

He says he wants to “radically change the focus of health and social care onto prevention”. 

Last month I wrote an article that pre-empted Hancock’s policy paper, published yesterday. I wrote critically about a number of his proposals in Government plans to use your phone and online data to police your lifestyle and predict ‘threats’ to your health.

Hancock has called for an increase in ‘social prescribing’ – referring patients to classes and community groups – in a bid to “shift the balance” away from GPs ‘automatically prescribing drugs for many illnesses.’  socialprescribing

He said in September“The evidence increasingly shows that activities like social clubs, art, ballroom dancing and gardening can be more effective than medicines for some people and I want to see an increase in that sort of social prescribing.” 

In practice, social prescribing means that GPs, nurses and other healthcare practitioners work with patients to identify non-medical opportunities or interventions that will help, improving support and the wider social aspects of their lives. The services that patients can choose from include everything from debt counselling, support groups, allotments and walking clubs, to community cooking classes and one-to-one coaching.

Both evidence and commons sense suggests that social prescribing may be particularly appropriate and beneficial for isolated, marginalised groups. It is a needs-led community provision that supports and enhances psychosocial health and wellbeing. However, Hancock seems to think it may be used as a substitute for medicine. 

The psychosocial approach has already been used to cut the budget for disability welfare support, with some tragic consequences. Now, the same approach in the form of social prescriptions is being proposed to cut the NHS bill. The University of York has already produced research to show that there is little good quality evidence that social prescribing is cost-effective

The Conservative government has made a link between social prescriptions, cost-cutting and (as I deeply suspected) as a mechanism of extending behavioural modification (euphemistically called “nudgingby the government’s team of behavioural economists and decision-making “experts”).

Nesta, who now partly own the government’s Behavioural Insights Team (the Nudge Unit) are of course at the forefront of promoting social prescriptions among medical professionals, firmly linking what is very good idea with very anti-democratic Conservative notions of behaviour change, citizen responsibility and small-state ideology. So, it’s no longer just about helping people to access a wider range of community-based services and support, social prescribing has also places strong emphasis on “encouraging patients to think about how they can take better care of themselves.” 

Nesta may have a whopping ‘cognitive bias’ here. A ‘perverse incentive’. It’s called the ‘profit’ incentive.

The same (bio)psychosocial model has been used to disingenuously trivialise and euphemise serious physical illnesses, implying either a psychosomatic basis or reducing symptoms to nothing more than a presentation of malingering tactics. This ploy has been exploited by medical insurance companies (infamously by Unum Provident in the USA) and government welfare departments keen to limit or deny access to medical, social care and social security payments, and to manufacture ideologically determined outcomes that are not at all in the best interests of patients, invalidating diagnoses, people’s experience and accounts, and the existence of serious medical conditions

Unum was involved in advising the government on making the devastating cuts to disabled people’s support in the UK’s controversial Welfare Reform Bill.

Hancock said in his speech at the International Association of National Public Health Institutes: “Prevention is also about ensuring people take greater responsibility for managing their own health.

“It’s about people choosing to look after themselves better, staying active and stopping smoking. Making better choices by limiting alcohol, sugar, salt and fat.”

Hancock claims it is not about “patronising” patients, “It’s about helping them make better choices, giving them all the support we can, because we know taking the tough decisions is never easy.”

“In the UK, we are spending £97bn of public money on treating disease and only £8bn preventing it across the UK”.

“You don’t have to be an economist to see those numbers don’t stack up.”

public spending

No, the numbers don’t stack up. Approximately 14 billion is spent by the Department of Health on things like public health initiatives (which aim to improve people’s health so they don’t need to use the NHS as often), education, training, and infrastructure (such as IT and building new hospitals). 

The Conservatives said in their 2015 election manifesto they would provide £8 billion in government, and expect another other £22 billion in savings from the NHS. The Nuffield Trust said this still left unanswered questions on funding:

“£8bn is the bare minimum to maintain existing standards of care for a growing and ageing population …

“improving productivity on this scale [£22 billion] would be unprecedented”

The Conservative government followed through on the commitment and then started claiming it was giving £10 billion, providing the NHS what it asked for, and more.

In their 2017 election manifesto, the Conservatives said they would increase NHS spending by at least £8 billion in real terms over the next five years, and increase funding per head of the population for the duration of the parliament.

Last year the think tanks said there would be a £4 billion gap in health spending in 2018/19 alone, but the £1.9 billion provided by the government at the end of last year meant that “around half of the minimum gap we calculated has been filled.”

They said even based on the government’s current spending plans there is likely to be a spending gap of over £20 billion by 2022/23. 

Approximately 44 % of NHS trusts—which provide secondary care to patients who’ve been referred there by a GP—were in the red in 2017/18. The figure was 65% just among acute hospital trusts—which make up the bulk of NHS trusts across England.

Collectively they finished 2017/18 with a deficit of around £960 million.

In this context, social prescriptions are used to maintain the status quo, and are likely to be part of a broader process of responsibility ascription – based on the traditional Conservative maxim of self-help, which is used to prop up fiscal discipline and public funding cuts, the extensive privatisation of public services, defense of private property and privilege, and of course, the free market. The irony of the New Right, neoliberal, paternalistic libertarianism is that the associated policies are not remotely libertarian. They are strongly authoritarian. It’s a government that doesn’t respond to public needs, but rather, it’s one that pre-determines public interests to fit within an ideological framework.

Theresa May has pledged millions of pounds to use Artificial Intelligence (AI) to “improve early diagnosis of cancer and chronic disease.” In a speech delivered earlier this year, May also called for the industry and charities to “join the NHS in creating algorithms that can predict a patient’s care requirements based on their medical records and lifestyle information.” 

The government believes that early intervention would provide “less invasive, more affordable and more successful care than late intervention,” which they claim “often fails.”  

While the government has assumed that the unmatched size of the NHS’s collection of data makes it ideal for implementing AI, many are concerned about data privacy.

Importantly, May’s proposal would (once again) allow commercial firms to access NHS data for profit.

In April 2018, a £1bn AI sector deal between UK Government and industry was announced, including £300million towards AI research. AI is lauded as having the potential to help address important health challenges, such as meeting the care needs of an ageing population. 

Major technology companies – including Google, Microsoft, and IBM – are investing in the development of AI for healthcare and research. The number of AI start-up companies has also been steadily increasing. There are several UK based companies, some of which have been set up in collaboration with UK universities and hospitals.

Partnerships have already been formed between NHS providers and AI developers such as IBM, DeepMind, Babylon Health and Ultromics. Such partnerships have attracted controversy, and wider concerns about AI have been the focus of several inquiries and initiatives within industry, and medical and policy communities. 

Last year, Sir John Bell, a professor of medicine at Oxford university, led government-commissioned review. He said that NHS patient records are uniquely suited for driving the development of powerful algorithms that could “transform healthcare” and seed an “entirely new industry” in profitable AI-based diagnostics. 

Bell describes the recent controversy surrounding the Royal Free hospital in London granting Google DeepMind access to 1.6m patient records as the “canary in the coalmine”.

“I heard that story and thought ‘Hang on a minute, who’s going to profit from that?’” he said. 

Bell gave the hypothetical example of using an anonymised data for chest radiographs to develop an algorithm that eliminated the need for chest x-rays from the ‘analytical pathway’.

“That’s worth a fortune,” he said. “All the value is in the data and the data is owned by the UK taxpayer. There has to be really serious thought about protecting those interests as we go forward.”

However, Bell highlighted a “very urgent” need to review how private companies are given access to NHS data and the ownership of algorithms developed using these records.

Hancock, the recently appointed health secretary, is now planning a “radical” and highly invasive system of “predictive prevention”, in which algorithms will use detailed data on citizens to send targeted “healthy living messages” to those flagged as having “propensities to health problems”, such as taking up smoking or becoming obese. 

People’s medical records will be combined with social and smartphone data to predict who will pick up bad habits and stop them getting ill, under radical government proposals. Of course this betrays a fundamnetal assumption of the government: that illness arises because of  bad “lifestyle choices.” 

In the policy paper released yesterday, Hancock says “Prevention means stopping problems from arising in the first place; focusing on keeping people healthy, not just treating them when they become ill. And if they do, it means supporting them to manage their health earlier and more effectively. 

This means giving people the knowledge, skills and confidence to take full control of their lives and their health and social care, and making healthy choices as easy as possible.” 

And: “Last year, over 20 million people used the NHS website. Over the next ten years, digital services will become even more widespread, and the first point of contact for many. The management of health will move out of clinical settings, and into the hands of people. Devices and applications will provide guidance and support around the clock.”

Hancock also said that Public Health England will look at “harnessing digital technology” as a form of “predictive prevention”, potentially leading to targeted health advice for people based on their their location and lifestyle. 

His focus is on “improving health, reducing demand for public services and supporting economic growth.

And: “Predictive prevention will transform public health by harnessing digital technology and personal data – appropriately safeguarded – to prevent people becoming patients. The availability of public data, combined with the existing understanding of wider determinants of health, means we can use digital tools to better identify risks and then help the behaviours of people most in need – before they become patients. 

“Historically, public health has dealt with populations as a whole – a one-size-fits-all approach. The power of predictive prevention comes from enabling people to look at their health in the context of their own life, their own circumstances, and their own behaviour. “

“This means moving beyond a simply clinical view of a body system or disease. It means envisioning a world where everyone can understand their own risks, both in their genetic make-up and from their personal behaviour. We will be able to empower people to make positive changes – and not always in ways we have traditionally thought about.”

Whenever the Conservatives use words like ’empower’, ‘help’ or ‘support’, I worry, because the ideological context of neoliberalism changes the political meaning of these Orwellian Conservative signpost words. Similarly, when Conservatives use the word ‘sustainability’, it is invariably with a view to making catastrophic funding cuts to social safety net provision and wider public services. 

Hancock says more than once: “The ambition is to prevent people becoming patients.”

Inevitably, he came to : “We want to ensure better integration between health and employment support services to help people with health conditions to enter and stay in work. This means ensuring people receive work-related advice and support within the NHS as part of making work a health outcome; on the basis that good work is good for health.” The basis is unverified.

The government conducted a survey in 2011 that showed if people believed that work is good for them, they are less likely to take time off. There is no evidence that demonstrates work is good for health. There is evidence that suggests people who are well enough to work generally do. It is not possible to ‘make’ work ‘a health outcome’. People are either healthy enough to work or they are not. The fact that healthier people work on the whole does not make work ‘good’ for people’s health. Poverty is historically linked with poor health. In work poverty has risen over the last decade. Having a job is no guarantee of escaping poverty or ill health. 

Job coaches are already asking GPs to refer patients to them, and have even suggested that GPs should make sick notes conditional on patients making an appointment with a work coach. 

Hancock’s proposals hint at a plan to extend conditionality in health care. 

Helen Donovan, Professional Lead for Public Health at the Royal College of Nursing, said: “We welcome the fact that the Health Secretary is making prevention a priority, and clearly recognises that a focus on public health will keep people healthier for longer and save the NHS money and resources in the long run.

“But Matt Hancock must realise his plans will start at a disadvantage as local authorities struggle with planned cuts to public health budgets of almost four per cent per year until 2021. While it’s clear he sees that prevention isn’t an optional extra, we need to see properly funded, accountable services delivered by a fully staffed nursing workforce backed by adequate resources. Disadvantaged areas emerge worse off without these vital services with life expectancy and the poorest bear the brunt of underinvestment in public health.”

Jonathan Ashworth MP, Labour’s Shadow Health and Social Care Secretary, said: “The Tories have imposed swingeing cuts to public health services, slashing vital prevention support such as smoking cessation services, sexual health services, substance misuse services and obesity help.

“In local communities, years of cuts and failed privatisation have resulted in health visitor and school nurse numbers falling, whilst children are losing out on the key early years health interventions they need.

“Many of the aims announced today are laudable but the reality is currently a further £1bn worth of cuts to health services including public health are set to be imposed by this Government next year.”

He added that unless the cuts were reversed, the green paper (planned for next year) would ”be dismissed as a litany of hollow promises”.

Simon Capewell, a professor of public health and policy at Liverpool University, said the minister was right to emphasise the need for effective prevention of epidemics such as obesity, type 2 diabetes and dementia.

But he added: “We must recognise the huge power of our lived environment, and avoid naively just focusing on ‘personal responsibility’ and ‘individual choices’. People do not ‘choose’ obesity or diabetes or cancer. They have just been overwhelmed by a toxic environment.”

The big drop in the last decade in the number of  UK citizens who smoke showed that firm, consistent government action was the best way to boost public health, Capewell said.

He added: “Mr Hancock can celebrate previous health successes with tobacco control. That success was built not on victim blaming, but on strong tax and regulation policies to reduce the ‘three As’ of tobacco affordability, availability and acceptability.”

Ministers need to take similarly tough action now against “the production of the commodities which harm people’s ill health, including junk food, cheap booze and fixed-odds betting terminals,” he said.

Hancock has of course denied that the government’s austerity programme had an impact on public health. In an interview for the BBC’s Today programme Hancock said: “The biggest impact on your health from the economy is whether or not you have got a job, and there are record numbers of jobs in this country.”

This of course is utter rubbish. If Hancock’s magical thinking was true, health in the UK would have dramatically improved over the last few years in line with ‘record employment levels’. But it hasn’t. The Conservatives are a party that prefers dogma over evidence, ideology over public services and the pseudopsychology of nudge over policies that meet public needs. 

Several health organisations have highlighted that local councils in England have had to cut their public health budgets in recent years, and will do so again next year, because Hancock’s department of health and social care has reduced their grants to divert more money to frontline NHS services. Many local councils have delivered preventative health programmes, but are now finding it increasingly difficult to deliver the statutory services. 

Jonathan Ashworth, the shadow health secretary, heavily criticised Hancock’s remarks. “From telling people to stand up in meetings to now lecturing people about their habits, while cutting £1bn from health services, isn’t a serious plan for improving the health of the nation,” he said.

public spending

Over the weekend Theresa May said the Conservatives “are now the natural party of the NHS” and said the Government was putting the public health system, created 70 years ago, on a path to “prosper for another 70 years and more”. That is most certainly an empirically unverified statement. 

It’s utter rubbish.

Matt Hancock Health secretary at his office

Update
Related  

Demedicalising illness and deprofessionalising healthcare: Rogue company Unum’s profiteering hand in the government’s work, health and disability green paper

GPs told to consider making fit notes conditional on patients having appointment with work coach

Government plans to use your phone and online data to police your lifestyle and predict ‘threats’ to your health

Cash for Care: nudging doctors to ration healthcare provision

Rationing and resource gatekeeping in the NHS is the consequence of privatisation

 


My work is unfunded and I don’t make any money from it. This is a pay as you like site. If you wish you can support me by making a one-off donation or a monthly contribution. This will help me continue to research and write independent, insightful and informative articles, and to continue to support others.

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Neil was forced to spend 6 hours applying for Universal Credit just after having surgery for brain cancer

Neil MacVicar is in remission from a brain tumour (Photo: Fabio De Paola)

Neil MacVicar is now in remission from a brain tumour (Photo: Fabio De Paola) 

Neil MacVicar was diagnosed with cancer at the age of 25 in December 2016. Doctors found a tumour the “size of a plum” on his brain.

Just twelve days after neurosurgery to remove the growth, when he should have been recovering and preparing for gruelling radiotherapy, Neil was forced to go to the Jobcentre to sign on for Universal Credit.

The application can be difficult for claimants in good health. For a cancer patient  struggling with exhaustion and confusion from an operation, it was nearly impossible. It took Neil six gruelling hours in total to complete his application.

He was staying with his family in Inverness at the time, and Neil cannot understand why, given his circumstances, he was made to endure that and why the Jobcentre could not have obtained the information from his doctors.

He is now in remission after successful surgery and treatment, and says he was let down by the “bizarre” system. 

Neil told inews :“They had me sitting in the actual Jobcentre for a little bit trying to fill in the forms. Then I went home and had to do it. My concentration was all over the place so it took me absolutely ages. I don’t understand why they couldn’t just get that [information] from the doctors.”

“I thought I was being perceived as scamming the system. I had cancer. I felt really let down to be honest,” he says.

It took Neil a while to realise there was something wrong with his health. He moved to London from Scotland seven years ago, was working hard as a bar manager at the time. The work was “stressful work with long hours” but he started to experience dizziness, which he suspected was related to an earache. With his symptoms getting worse, he went to hospital while visiting his family in Inverness, on Scotland’s northeast coast.

He said: “Doctors realised I had a brain tumour the size of a plum. They rushed me through to Aberdeen for surgery. And then a week or two later they phoned me to say it was cancer. It wasn’t a benign tumour.”

Knowing he would have to stay in Scotland for the duration of his treatment, Neil decided to keep renting his room in Islington, northwest London. “I thought I would be bouncing back and returning to my normal life relatively quickly.”

Before he began six weeks of aggressive radiotherapy, Neil tried to sign on to Universal Credit. Following the stressful and lengthy application process, his anger and disappointment only intensified as he had to wait about six weeks for his first payment to come through. When his money did arrive, Neil was shocked at the amount: £780. It covered his rent and bills for his room in London but left him with barely anything to live on day-to-day. 

“I phoned them up to say there must be mistake. I was kept on hold for an hour at a time when I was going through my radiotherapy only to be told because I’m 25, I’m not an adult so I should just move back in with my parents. And then they told me it was my fault for living in Islington and that it’s expensive there and I could just move somewhere cheaper.

He added: “I’m very independent. I’ve lived by myself since I was 19 so hearing that I’m not an adult was absolutely insane to me. I was old enough to get married, buy booze and serve in the army but [I wasn’t considered an] adult [to get] benefits. It really got me down.”

After recovery over a few months, Neil moved back to London in June 2017 and continued to receive Universal Credit. He was eager to get back into work but could only do a part-time job because the cancer had left him with severe fatigue. 

“There was no support there. I kept saying to my work coach [Jobcentre employees who help claimants move into employment] I was desperate for work. She didn’t lift a single finger to help me find anything. Nothing at all. Which has really pissed me off to be honest.”

Neil, now 27, has found a job as a support worker for a charity which helps people with mental health problems receive their benefits. He says his experience with Universal Credit has left him feeling “down, angry and upset”. 

“I had multiple times when I was in tears because of it. On top of everything; the amount of shit I had to go through with the cancer and surgery.”

He added: “I think if I didn’t have the support network of my parents and friends I’d either be homeless or dead and that’s the reality. As a cancer patient, every single bit of this has penalised me for trying to move forward in my life. There has been no help or support [from the Jobcentre], only from charities which are inundated with people struggling with Universal Credit.”  

Macmillan Cancer Support’s chief executive Lynda Thomas said: “People with cancer should be able to focus their energy on their health, not worrying about how to make ends meet when they are too unwell to work.”

“It is unacceptable to force patients to risk infection at Jocentres, log onto computers from hospital and wait more than a month for vital financial support, even at the end of their lives.

“The system is failing people with cancer and we urge the Government to fix this benefit, before tens of thousands more vulnerable people are put at risk of hardship.”

A Department for Work and Pensions spokesperson said: “Universal Credit is a flexible benefit, and we can reschedule appointments, if people make us aware that they are unwell.

“We’re committed to ensuring that people with health conditions get the support they’re entitled to. Decisions on PIP are made following consideration of all the information provided by the claimant, including supporting evidence from their GP or medical specialist.”

The Department seem to disregard the fact that sometimes people are simply too ill to provide an indifferent wall of bureaucracy with endless evidence that they are ‘really’ ill. 

Anyone in need of welfare advice can call Macmillan’s free support line on 0808 808 00 00 or visit www.macmillan.org.uk 

 


My work is unfunded and I don’t make any money from it. This is a pay as you like site. If you wish you can support me by making a one-off donation or a monthly contribution. This will help me continue to research and write independent, insightful and informative articles, and to continue to support others.

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MPs ‘left with no option but to vote down’ unscrutinised new Universal Credit regulations

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Over recent months, MPs on both sides of the House of Commons have pleaded with the Government not to go ahead with transferring claimants from existing benefits to the much troubled Universal Credit until it can guarantee that every claimant would be migrated safely onto the new benefit and none would be left without money. 

Today (4 November) the Commons Work and Pensions Select Committee is publishing correspondence with Alok Sharma MP, Minister of State for Employment (see below), about the Government’s plans for moving people claiming existing benefits onto Universal Credit, ahead of new rules on so-called “managed migration” being laid in Parliament. The Government announced in October that “managed migration” of claimants on to Universal Credit, originally intended to begin in early 2019, would be pushed back.   

The Government’s original plans have been widely criticised by front-line charities and others, with predictions that vulnerable people could be plunged deeper into poverty and even that some people entitled to benefits could be left with no income whatsoever. The rules have been subject to a review by the Social Security Advisory Committee (SSAC), who presented their report to DWP earlier in the autumn.

Minister refuses request to share new rules on Managed Migration

In a hearing on 18 October, the Committee asked the Minister to commit to sharing the new version of the rules with the Committee before it was formally given to Parliament, to allow the Committee to determine whether the serious concerns already raised about the plans, including in evidence to the SSAC, have been addressed. In the response being published today the Minister refuses that request. 

The Chair has urgently written again to the Minister (also attached), saying: “Given the strength of the concern about the draft regulations published in June… we can only hope that the revised version has changed beyond recognition […] if the Government has accepted the SSAC’s advice, and has fully addressed the very serious concerns expressed to the SSAC during its consultation, then our scrutiny could be very quick and need not cause any significant delay. Might I therefore ask please whether you could urgently reconsider this decision?”

Chair’s Comment

Comment from Work and Pensions Committee Chair Frank Field MP:

“Having got it so disastrously wrong with its first attempt, you’d think that the Government would want to make sure its plans to move vulnerable people onto Universal Credit stood up to robust scrutiny. Instead, it is choosing to push these regulations through Parliament with no chance for MPs to make amendments. 

That hardly inspires confidence that it has really made the changes needed to ensure that its actions won’t plunge people deeper into poverty. If its new plans don’t have enough safeguards to protect the vulnerable, then MPs will be left with no option but to vote them down.”

See: 

Image result for scrap universal credit


My work is unfunded and I don’t make any money from it. This is a pay as you like site. If you wish you can support me by making a one-off donation or a monthly contribution. This will help me continue to research and write independent, insightful and informative articles, and to continue to support others.

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Universal Credit is set to cost billions more than legacy benefits, says government’s spending watchdog

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Despite the widespread concerns about the financial hardships that Universal Credit has created for many people , the government’s official spending watchdog says that the Conservative’s flagship policy will, nonetheless, cost the UK billions more than the legacy benefits system over the next five years. 

In its response to the Autumn Budget, the Office for Budget Responsibility (OBR) changed its previous prediction in March 2018 that the government’s controversial welfare overhaul will save public money. Instead, the OBR now forecasts that Universal Credit will cost ‘the taxpayer’ £7.1bn more than the current system between 2019/20 and 2023/24.

That amount also includes new funding for the programme announced by chancellor Philip Hammond on Monday in response to the serious concerns raised by MPs about the impact Universal Credit is having on people.

However, the OBR added that even without these measures, which include an extra £1bn for transition support and a £1.7bn-a-year plan to raise the work allowance threshold for some claimants, Universal Credit would have a net cost of £1.9bn over the next five years.

Perhaps an analysis of the costs of the administrative and delivery framework would be useful. 

The OBR say: “On a pre-measures basis UC is now projected to be more expensive than the legacy system would have been from 2019-20 to 2022-23, having been less expensive (i.e. generating a net saving to the Exchequer) in our March forecast. This reflects many changes, some down to revising key assumptions that can now be tested against outturn data relating to the 1 million or so cases now on UC.” 

In its Economic and Fiscal Outlook based on the Autumn Budget, the OBR said: “Our pre-measures forecast revisions were sufficiently large to push our estimate of the effect of [Universal Credit] on welfare spending from a net saving to a net cost in most years – the first time that it has been shown as a net cost on average since our March 2015 forecast.”

The watchdog added :“Once Budget measures are factored in, the marginal cost moves significantly higher.”

The high cost of Universal Credit indicates that the political motivation behind this radical reform is purely ideological, rather than being based on any economic necessity. ‘Making work pay’ is about punishment and discipline – ultimately it is about driving people into any work available, regardless of job security and conditions, regardless of whether the wages meet the costs of living.

Meanwhile in work poverty is growing significantly. Deregulated, supply side labour market policies drive wages down. Reducing welfare support creates a desperate reserve army of labour who have absolutely no collective bargaining powers to improve work conditions. 

Other comments of interest include: “The Department for Work and Pensions (DWP) is subject to ongoing legal challenges. We asked the Government whether there is a detailed central list of ongoing DWP legal challenges and the likelihood of losing them, and why it takes a different approach to recording these DWP contingent liabilities than it does to tax-related legal challenges recorded in HMRC’s departmental accounts.

“The Treasury stated that it is working to improve the reporting and managing of DWP’s legal cases in accordance with steps set out in its 2018 Managing Fiscal Risks report.”

The OBR report also confirms that disabled people in receipt of severe disability premia will not be moved onto Universal Credit until provision is made to ensure the premia are integrated to ensure people on legacy benefits such as Employment and Support Allowance are not left worse off through migration or through a change of circumstance that means a new claim has to be made. This follows a court ruling that the loss of disability premia is unlawfully discriminatory. 

The court defeat for the government indicates once again how unfit for purpose Universal Credit is. Rather than being the ‘simplified’ system as promised, the administration of the welfare provision has become subject to a series of post hoc amendments because of the original model’s incorporated and systemic abuse of people’s human rights and violation of equality legislation. These are being uncovered by ongoing legal challenges.

Image result for Universal credit is coming


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Council told me to submit an FoI for the details of my housing benefit award and alleged DHP ‘overpayments’

Image result for Discretionary housing payments

Last year I fell into difficulties because my housing benefit was decreased. I struggled to make up the shortfall to pay my rent. I also had to pay council tax as my council tax benefit was reduced. I made an appointment with my local council welfare service, who advised me to claim Discretionary Housing Payments. They supported me in working out my monthly expenses and they found that I was over £200 a month short to meet my basic living costs, including rent. I was very ill at the time with a severe flare up of lupus and my mobility was extremely poor. 

The welfare service contacted occupational therapy on my behalf, and they organised an appointment for an assessment, and subsequently, for the provision of some aids and adaptations in my home because I often struggle getting about. The welfare service advised me to claim Personal Independent Payment (PIP) and supported me with my claim. I had such a distressing experience claiming Employment and Support Allowance (ESA) in 2011, having to appeal the decision, then almost immediately after winning at tribunal, I was sent for a re-assessment, that I had put off claiming PIP for six years, even though I needed the support very much. The distress and strain caused by each assessment, including the one for PIP, has exacerbated my illness.

The housing team decided that Discretionary Housing Payment (DHP) would be awarded for a year. This is a fairly standard award length. The DHP was to help cover the extra cost I had because of the deductions being made to my housing benefit while my son was at home. He took six months out from university because in February 2017 I developed pneumonia and sepsis. I was very seriously ill and almost died because I developed severe sepsis and septic shock. My son supported me after I came home from hospital, while I recovered, which took several months.

When I was awarded PIP, my housing benefit was amended and an increase in my award was backdated to the date of my claim for PIP. Because my son was staying at home, deductions had been made – the bedroom tax – because he was classed as a ‘non dependent’, even though he had no income for that period, as he is a student. The council tax charge arose because of the same reason. Although my rented property is a private one, my local council nonetheless call the non dependent deduction a bedroom tax. 

Councils are not allowed to make deductions for non dependents from people who have a PIP award with the daily living component. I came across this rule on the government site. I notified the council and explained the rule, as they didn’t seem to know about it. I was then reassessed and awarded the money that was deducted from my housing benefit for the bedroom tax, and the council backdated the amount they repaid to when I first made my PIP claim, which was from late July to April, 2017.

I received a letter explaining how my housing benefit had been worked out again. I then received a letter from the Discretionary Housing Payments section of the council, saying I had been overpaid DHP from April to July. This is because my housing benefit had increased and the increase was backpaid.

I was told I had to repay the DHP. It was deducted from my housing benefit without further discussion – leaving me short again for my rent and defeating the objective of DHP. I had claimed DHP early last year because of the bedroom tax shortfall. 

I was not informed about the rule that councils cannot make deductions for non dependents if someone is awarded the daily living component of PIP, I had to find that out myself. Nor did the council indicate that if my housing benefit was increased by the housing benefit section retrospectively, that would mean I may have to repay my DHP. I was not informed that if the housing benefit sector had made an error, I may be expected to repay the DHP awarded. However, the error occured through no fault on my part, so I ought to have challenged the claim of overpayment, but I did not know the rules about this at the time.

I was not informed at the time I made my claim for DHP that if I got my PIP award, my housing benefit would increase and that the increase would be backdated to the date of my PIP claim. It’s also reasonable to assume that the housing benefit office would have taken into account that I had a DHP award when they paid me the money for the  deductions they had made over that period. 

Money was taken from my housing benefit to recover the DHP, which left me in hardship again every month. This defeats the whole stated purpose of DHP awards.

However, I have since learned that DHP ‘overpayments’ are only deemed as such in certain circumstances, which are not applicable in my case. I should not have been asked to repay my DHP.

I also learned that deductions for overpayments CANNOT be made from ongoing housing benefit awards, Universal Credit awards or any other benefit. Housing benefit and DHP are seperate awards.

The council have violated rules that are clearly stated on the council’s own website as well as those set out in the government guidance for DHP

In a document called Discretionary Housing Payments Guidance Manual on the government website, it says: “A DHP cannot be recovered from on-going HB or UC. This is unlike HB overpayments where there is a regulatory provision to allow recovery from on-going HB. There are also no provisions for the recovery of overpaid DHPs from other prescribed benefits.”

It also says:  “You can only recover a DHP if you decide that payment has been made
as a result of:

 a misrepresentation or failure to disclose a material fact by the claimant (either fraudulently or otherwise), or
 an error made when the application was determined.”

Neither of those criteria apply. When the application was determined, I was not in receipt of PIP. The bedroom tax and council tax deductions were being made, and that  predated my application for DHP and was not through any fault of my own. The non dependent deductions continued until after I had notified the council of my PIP award, and I had to inform them of the rule about PIP daily living component and non dependent deductions myself before they reassessed my claim, because I read the rules about this on the government PIP website last year. 

I was then awarded the total amount that had been deducted for a ‘non dependent.’ I had to ring several times before the council tax I had paid was given back. The council had not even considered repaying me those deductions. I was not informed at any time that I may be asked to repay any of the DHP award, and I think it is fair to assume that the housing benefit department took the DHP award into account when they made their decision to pay me the deductions they had taken, and when they calculated the amount I was owed. 

The DHP section claimed I was overpaid despite the fact that this doesn’t tally with government guidelines, which outline what circumstances may be defined as an overpayment. None of the criteria applied to the circumstances of my claim. The guidance states that if the claimant has not contributed to an error, then they should not be asked to repay any DHP. 

The money was deducted from my housing benefit award from towards the end of last year, and throughout most of this year – I had to ring and ask for the weekly deductions to be reduced early this year as they were causing me hardship. The minimum deduction the DHP section said they could make was £10 per week, and they had been taking £20 per week.

It seems the council are not aware of the rules that apply to non deductions and PIP, or to DHP awards and the rule that says ‘recovery’ cannot be made by making deductions to ongoing housing benefit/Universal Credit. But it is too late for me to query or challenge the recovery as all of that DHP award period has now been taken from my housing benefit. I only found the government DHP guidelines this year, because another problem has arisen.

It seems that people who claim any support have to become welfare specialists in order to understand the rules and guidelines because many administrative authorities don’t seem to know them. Or perhaps they know about them but are reluctant to apply them until they have to.

Yet today I checked the council’s website and found a section on DHP administration, and the rules I have cited here are clearly written in their own guidlelines. 

It gets worse: another error

From April this year, the council had been making more ‘non dependent’ deductions for my other son who, they now tell me, was assumed to have left home because he was in university. That, they told me, left me with a ‘spare room’. The council did not tell me they had reduced my payments, or provide any explanation. The DHP section were also making deductions from my housing benefit, though my award from DHP was ended at the time. That is not supposed to happen according to the government and my local council’s rules.

The government guidelines say that if there is a deemed overpayment of DHP, it cannot be deducted from an ongoing housing benefit or universal credit award. I did not know this at the time, and the deductions continued until September, when I rang the council to ask why my housing benefit payments were so low, leaving me with a huge shortfall to find for my rent. I did know about the DHP deductions, but had assumed that the council were acting according to the rules. They told me that my son had left home and gone to university. I explained that he had not. Again. 

My youngest son left university last September. While he was at university, he returned home out of term times, and was therefore legally classed as living at home. 

The council had previously assumed my older son had left home too when he first went to university, but I found the rule on the government website that says if students return home – out of term times, for example – then they are legally classed as living at home and non dependent deductions cannot be made in these circumstances.

I challenged the decision to reduce my housing benefit at that time, because the council benefit office notified me of their intention. They ended the deductions for the ‘spare room’, because I provided evidence that my son returned home outside of term times.

However, I had NO notification about the decision to deduct money from my housing benefit for my younger son – a ‘bedroom tax’ – or any explanation why my benefit was reduced. He returned home out of term times (so was legally classed as living at home) and anyway, the dates that the housing benefit office applied the bedroom tax, my son had already left university and returned home permanently. As I am in receipt of PIP daily care component, they cannot make deductions for a ‘non dependent’ from my housing benefit. 

I challenged the underpayments and was paid the money that was deducted, again, as it was the councils’ mistake because they did not notify me about why they were making deductions, and gave me no opportunity to challenge the decision.

With the recent letter explaining how the reimbursment had been worked out from the housing benefit section, there was a notification from DHP section dated 25 September this year, thanking me for a claim I never made this year – they had retrospectively made an award and backdated it to last year, which I thought was very odd at the time I got the bundle of documents in the post.

Now, low and behold DHP section are claiming once again that I have been ‘overpaid’ for the period they retrospectively made the award (my rent allowance was more than £60 a month short at the time leaving me with more than £80 per month to find for my rent. DHP administrators now say they want more than half of what I was reimbursed by the housing benefit section back. However, as far as I was aware, that reimbursement was my shortfall in housing benefit, FROM the housing benefit office, which is not the same thing as DHP. The council can’t tell me what deductions had been made by DHP section and what deductions were made for the bedroom tax from the beginning of April to September this year

Going through my bank statements, I can see something isn’t right with what the DHP section are claiming because it doesn’t seem that I was paid the DHP for the most recent period. The amounts I received for housing costs were way too low, even accounting for the deductions for my son, made in error on the housing benefit sections’ part. And the housing benefit section would surely not reimburse DHP payments as they are seperate thing. Yet DHP section claim I have been ‘paid twice’. To complicate things further, DHP were making deductions from my housing benefit over some of this period too for the previous ‘overpayment’. 

I went through the housing benefit amounts I was originally paid on my bank statement over the last year and a half. The amounts I got over the period varied. Up until late September, 2017, it was clear that I was getting DHP, as the shortfall between my housing benefit and rent was £50. Then my overall housing benefit amount dropped by a further £20 fortnightly. This is the period that DHP now claim I was ‘overpaid’, yet I can’t see any evidence they actually paid me my award over this time span on my bank statement.

It’s very confusing and the lack of transparency regarding payment details means that I am struggling to work out exactly what was deducted for bedroom tax, what DHP were deducting at the time, and what they were actually paying me, since they claim they were making payments.

I asked the council yesterday for a breakdown of information regarding this matter yesterday and I was advised, unbelievably, to submit a Freedom of Information (FoI) request.

I’m not sure that people can submit FoIs about themselves. I think he probably meant meant a Data Subject Access Request (SAR), on reflection. However it should not be down to me to have to inform the council of the rules they ought to be following and to have to interpret badly worded advice. It’s reasonable to expect that council advisors give correct information and advice. 

In any event, bearing in mind that I have a month to submit my request for a review, and SARs often take quite a bit of time (and there’s no guarantee that the information will be provided), I think this was absolutely appalling advice. I asked for a precise breakdown of my payments and deductions – something you would expect a council to provide as a matter of transparency and as reasonable practice, and was subsequently presented with bureaucratic barriers to accessing that information.

The advisor I spoke to seemed as confused as me. I told him that DHP section are not permitted to make deductions from my ongoing housing benefit award, and he asked me where I got that information from. He then claimed that DHP can be deducted from a DHP award, implying that is what has happened. However, I pointed out that my DHP award had ended in April 2018 (it was awarded for one year) and DHP had been making deductions since then until October this year. He fell silent at that point. 

On my local council’s website, it says: “Where a DHP is found to have been overpaid the Benefit Service will consider whether it is appropriate to recover it in full, in part or not at all. As a general rule overpayments caused by official error will not be recovered, unless the customer caused or contributed to the error or was aware that too much was being paid.”

I did not cause or contribute to the error, nor was I aware if too much was paid or not.

It also says: “Notifications to the customer on overpaid DHP’s shall offer the opportunity
to seek a re-consideration.

63. Under no circumstances will recovery be sought for DHP from housing
benefit payments or universal credit payments due to the customer.”

So the advisor was claiming to be unaware of the council’s own rules, and furthermore, the council HAVE made deductions from my housing benefit award for DHP ‘overpayment’ from April to September this year when the council’s own rules state clearly that DHP administrators should not do so. 

It also says on the council’s website: “DHP overpayments can be written off in accordance with the authority’s current write off policy.”

If the council don’t consider that is an option in my case, as a disabled person who has been deemed ‘vulnerable’, it is highly unlikely they will for others in similar circumstances. 

I have now received an invoice for the amount DHP claims I was overpaid. However, the invoice has defined the overpayment as ‘housing benefit’, which is of course incorrect. I have been given 7 days to pay the amount. 

DHPs are discretionary and not subject to the statutory appeals mechanism, but they are subject to mandatory review.

Reading the government guidelines, the options available to DHP administrators are to a involve a debt collection agency and/or to take me to court if I don’t/can’t pay. I can’t pay. 

The council have told me to write a ‘complaint’. I was not informed of any further options.

However, reading the government guidlelines, my options are to ask for a review. If the matter is unresolved after that, I may then refer this matter to an independent council ombudsman. I can also ask for a judicial review. 

I shall be pursuing each of those options as necessary, if the situation remains unresolved.

I’m an ill and disabled person in receipt of PIP and the ESA support component. The council health and adult care section have assessed me and provided aids and adaptions in my home. The support I received from the council’s welfare service and occupational therapy has been excellent.

The housing benefit and DHP offices, however, have let me down very badly. My claim for DHP has actually increased my hardship in the longer term, and rather than mitigating the effects of government welfare reform and alleviating consequential hardships that affect vulnerable people, as intended, it has made my situation worse and caused me a significant amount of confusion, anxiety and distress.

I suffer with cognitive difficulties because of my illness, and trying to sort out mistakes made by the council and research the rules that the council ought to know about and apply has been both extremely stressful and difficult. I lost a night of sleep going through my bank statements yesterday. All of these events have seriously undermined my trust in the housing benefit and DHP offices, as these mistakes span over 2 years.

All of this very clearly highlights just how unfit for purpose government provision for ‘those most in need’ actually is.

I have two children, one still at university, both still live at home. I think that the political term ‘non dependents’ is a particularly nasty and authoritarian redefinition of adult children in poorer families, that undermines family bonds and attempts to redefine family relationships in terms of financial arrangements.

Neither of my younger sons can be defined as ‘non dependent’ because they still need a lot of financial and other kinds of support from me. I have a modestly sized 3 bedroomed house which has been adapted to meet my needs. There are no ‘spare rooms’, and my rent is actually relatively low. That said, the Local Housing Allowance (LHA) has been frozen for some years now, which means people like me have a large shortfall between the amount of housing benefit they can claim and the rent costs. 

The bedroom tax was a particularly spiteful Conservative policy aimed at the poorest citizens, and it has disproportionately affected disabled people. It’s a very authoritarian government that feels comfortable dictating the precise amount of living space some citizens are permitted, but then does not make any further provision to ensure that people can actually meet those mean spirited specifications. 

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Related

Discretionary Housing Payments Guidance Manual

 


My work is unfunded and I don’t make any money from it. This is a pay as you like site. If you wish you can support me by making a one-off donation or a monthly contribution. This will help me continue to research and write independent, insightful and informative articles, and to continue to support others.

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Paypal claim I am a ‘politically exposed person’ and have restricted my account

I logged into my paypal account and had the following message, completely out of the blue:

paypal limitation

I clicked on the PEP questions and got this:

politically exposed

I answered no because I don’t hold a position of political office, or ‘public trust’ and I’m not ‘associated’ with or related to someone in the public trust or polical office.  

I am, however, a member of a political party, like many other citizens. I have also been known to meet with MPs to raise and discuss issues with them. That does not make me a ‘politically exposed person.’

I briefly researched what a ‘politically exposed person’ is: “In financial regulation, “politically exposed person” (PEP) is a term describing someone who has been entrusted with a prominent public function. A PEP generally presents a higher risk for potential involvement in bribery and corruption by virtue of their position and the influence that they may hold.”

And: “While there is no global definition of a PEP, most countries have based their definition on the 2003 Financial Action Task Force on Money Laundering (FATF) standard, as for example the Swiss financial market regulator in 2011, which quoted it as “the international standard.” 

The FATF’s latest definition of politically exposed persons (PEP), revised from 2003, is as follows

  • Foreign PEPs: individuals who are or have been entrusted with prominent public functions by a foreign country, for example Heads of state or Heads of government, senior politicians, senior government, judicial or military officials, senior executives of state owned corporations, important political party officials.
  • Domestic PEPs: individuals who are or have been entrusted domestically with prominent public functions, for example Heads of State or of government, senior politicians, senior government, judicial or military officials, senior executives of state owned corporations, important political party officials. (Not all countries subscribe to the concept of domestic PEPs with respect to regulatory requirements/application of due diligence. For example, US law, specifically Section 312 of the USA Patriot Act and its implementing regulations provide for enhanced due diligence for SFPFs (Senior Foreign Political Figure) only, defined as: “a current or former senior official in the executive, legislative, administrative, military, or judicial branches of a ‘foreign’ government…a senior official of a major ‘foreign’ political party; and a senior executive of a ‘foreign’ government-owned commercial enterprise.)
  • Persons who are or have been entrusted with a prominent function by a state owned enterprise or an international organisation refers to members of senior management, i.e. directors, deputy directors and members of the board or equivalent functions.

Requirements for a PEP apply to family members or close associates, any individual publicly known, or known by the financial institution to be a close personal or professional associate.

None of these criteria apply to me.

As of January 2015 the UK’s PEP definition is identical to the 2003 FATF definition, i.e. without the 2012 update to include domestic PEPs; It is found in the Money Laundering Regulations 2007 Section 14(5)[9] A politically exposed person is considered any individual who fits any of the criteria listed below:

  • A foreign person who has held any time in the preceding year a prominent public function outside the United Kingdom, in a state or international institution
  • Members of courts of auditors or of the boards of central banks
  • Ambassadors, chargés d’affaires and high-ranking officers in the armed forces
  • Members of the administrative, management or supervisory bodies of state-owned enterprises
  • Heads of state, heads of government, ministers and deputy or assistant ministers
  • Members of parliaments
  • Members of supreme courts, constitutional courts or of other high-level judicial bodies

The definition explicitly excludes middle-ranking or more junior officials.

Apparently there are business screening tools available to “Screen your prospective clients against extensive global PEP lists.”  

There are a number of companies advertising for regulatory, financial and reputational risk screening.

‘Due diligence to uncover PEPs can be time consuming and requires the checking of names, dates of birth, national identification numbers and photos of clients against a reputable database of known PEPs, which usually contains over one million profiles.’

I should add at this point that I have this week had sudden inexplicable finance related problems. One is with a catalogue I have credit with (I needed a new cooker at the time, and other household items, which I have bought on credit) who have suddenly doubled the annual interest rate on my account, and justified this by claiming a ‘risk’ had come to light. They wouldn’t tell me what the ‘new risk’ was. I don’t have any other credit accounts, luckily, and have used the catalogue only when I have needed to replace essential household items for my family.

It’s probably unrelated, but I’m also suddenly battling with the council regarding an underpayment. They did reimburse me the amount last month thatthey had been deducting by mistake from my housing benefit over the last year. But now the council have this week retrospectively claimed that some of that money was Discretionary Housing Payment (DHP), and want more than half of the money they reimbursed me back.

The DHP, which I didn’t actually claim from the dates they say, was only awarded on the date I received the notification for the decision to reimbuse me the amount I was underpaid, and mysteriously backdated over a year. They are now claiming they paid that money at the time my rent was reduced for the reason the council claimed was behind the mistaken deductions. The deductions happened because the council decided without telling me that my son no longer lived at home. He was at university, but returned home out of term times. Legally that means he still lives at home. As it happens, he had eft university anyway and returned home permanently, for much of the period concerned.

The Council are now claiming – a month after this was sorted out and I was paid for the period of underpayment concerned that they had awarded DHP at the time, because they understood my son had left home. The period they claim they paid me for was last year. A notification for that didn’t arrive until I got a letter telling me the council had made a mistake and were going to reimburse me. The DHP notification letter was among the documents of how my benefit had been worked out. The letter thanked me for making a claim – that I never made for that period –  which I thought was odd at the time.

It’s bureaucratic bullshit that reminds me of the Thatcher era, when the DHSS kept ‘losing’ my ‘file’ and not paying me my unemployment benefit at a time when I was a lone parent with a baby, fleeing domestic violence, staying in a women’s aid refuge  – and a political activist. At that time, I had some major and inexplicable problems accessing any support that other people take for granted.

I do have to wonder how I could possibly even remotely be considered to be a ‘politically exposed person,’  given the definition. I have very little money. I don’t get a huge amount of donations on my site. The current balance on my Paypal site is £3.46.

This week I have had a few more donations than average because of an appeal for support to replace my laptop, which is broken, but that could not reasonably be considered a trigger for the current restriction on my account or of any suspicion of ‘corruption’.

The most I have ever had on my paypal balance is £100, minus the money that Paypal deduct. I often don’t check my balance for a week at a time or longer, because on average, I generally do not have very much on my balance.

I don’t get paid for the work I do. I would love to make a living from research and writing, but have been unable to so far. That won’t stop me from continuing doing what I do, though, providing I can stay connected to the internet, of course. 

People donate sometimes. Those donations of course are entirely voluntary, and they support me in researching and writing independent articles, as well as providing help for people who desperately need support. I support people with their PIP and ESA assessments, reviews and appeals. I also support people who contact me because they are profoundly distressed by of the consequences of government austerity policies. 

If simply being a person who cares very much about injustice, human rights, inequality and increasing poverty, and about how our society is organised makes me a ‘politically exposed person’, well, so be it.

 

Update

I contacted Paypal today and went through some security checks with them. I asked why I had been suspected of being a ‘politically exposed person’ and they replied that the company is obliged to carry out monitoring and checks. I asked them why they had decided they needed to carry out monitoring and checks on me, specifically, and they said they ‘could not say why’.

My account restrictions have now been lifted.


 

My work is unfunded and I don’t make any money from it. This is a pay as you like site. If you wish you can support me by making a one-off donation or a monthly contribution. This will help me continue to research and write independent, insightful and informative articles, and to continue to support others.

Until the issues on my account with Paypal have been resolved, I won’t be using their donation button. But you can contact me directly if you want to make a donation.

 

The budget will not alleviate inequality, poverty and hardship that government policies have created

Watch Jeremy Corbyn’s excellent response to the budget, while facing the braying, sneering, smirking government. 

Hammond is economical with copies of the Budget 

The Labour party have accused the chancellor Philip Hammond of breaking the ministerial code after opposition parties were not given a copy of the budget in advance. The code states that when a minister makes a statement to MPs in the Commons “a copy of the text of an oral statement should usually be shown to the opposition shortly before it is made”. The rules are that 15 copies and associated documents should be sent to the chief whip’s office at least 45 minutes before a statement. The government have frequently flouted these rules, prefering to follow the rampant authoritarianism protocol of avoiding scrutiny, transparency and above all, democratic accountability

However, a Treasury source claims that there was ‘no official rule’ that other parties should get an early look at budget measures. “We did not do anything differently from what we have been doing for the past 20 years,” the source said. I half expected him to add that the Ministerial Code isn’t really a code, but more a kind of ‘loose guideline’. 

The opposition is said to be considering a formal complaint. 

Austerity has not ended

Jeremy Corbyn accused the government of a U-turn on Theresa May’s party conference pledge that austerity was over. Hammond told MPs that austerity was “coming to an end”. The Labour leader replied: “The prime minister pledged austerity is over. This is a broken promises budget. What we’ve heard today are half measures and quick fixes while austerity grinds on.”

The Labour party also criticised income tax cuts, which it said would favour the better off and said there were no guarantees that government departments would not face further cuts. The Resolution Foundation have also concluded the same. 

Government rattles the Office for Budget Responsibility

The Office for Budget Responsibility (OBR), whose role, unsuprisingly, is to scrutinise the budget are also disgruntled because the government only handed over the final Budget policy measures on 25 October, a day late. This means the OBR hasn’t been able to check that the government’s sums actually add up.

The precise changes to universal credit came too late for the OBR to assess them properly, too. The budget red book says that the roll-out of universal credit is now scheduled to end in December 2023. It says:

In response to feedback on universal credit, the implementation schedule has been updated: it will begin in July 2019, as planned, but will end in December 2023.

But until recently, as this House of Commons library briefing (pdf) reveals, the roll-out was due to end in March 2023.

Officially the government says that, if the UK had to leave the EU with no deal, it could manage. But the OBR doesn’t share this view:

A disorderly one [Brexit] could have severe short-term implications for the economy, the exchange rate, asset prices and the public finances. The scale would be very hard to predict, given the lack of precedent.

The Press Association (PA) reports that the Labour leader said eight years of austerity has “damaged our economy” and delayed the recovery, adding the government has not abandoned the policy despite the chancellor’s latest spending pledges. The PA says:

Leading the response to the budget, Corbyn also said the proposals announced will “not undo the damage done” by the squeeze on spending.

He told the Commons: “The prime minister pledged austerity was over – this is a broken promise budget.

“What we’ve heard today are half measures and quick fixes while austerity grinds on.

“And far from people’s hard work and sacrifices having paid off, as the chancellor claims, this government has frittered it away in ideological tax cuts to the richest in our society.”

Corbyn added: “The government claims austerity has worked so now they can end it.

“That is absolutely the opposite of the truth – austerity needs to end because it has failed.”

Corbyn later said the “precious” NHS is a “thermometer of the wellbeing of our society”, adding: “But the illness is austerity – cuts to social care, failure to invest in housing and slashing of real social security.

“It has one inevitable consequence – people’s health has got worse and demands on the National Health Service have increased.”

Corbyn also condemned the “horrific and vile antisemitic and racist attack” in Pittsburgh, noting: “We stand together with those under threat from the far-right, wherever it may be, anywhere on this planet.”

The Labour leader criticised pay levels for public sector workers, adding: “Every public sector worker deserves a decent pay rise, but 60% of teachers are not getting it – neither are the police nor the Government’s own civil service workers.”

The economy is also being damaged by a “shambolic Brexit”, Corbyn added.”

Elements of the budget have revealed a Conservative party in ideological retreat. One of Jeremy Corbyn’s greatest achievements as leader of the opposition is the undermining of the neoliberal hegemony and his presentation of an alternative narrative and economic strategy. Personally I am glad that neocon neoliberal Francis Fukuyama didn’t get the last word after all. 

Over the last couple of years, the government have imported policy ideas and adopted rhetoric from the Labour party to use as strategic window dressing. Hammond announced an end to the government signing off on much-loathed private finance initiative contracts – something Corbyn had already promised. As a former Treasury advisor noted:

Originally introduced by John Major, and continued under New Labour, PFIs are essentially a way for the state to finance and then look after new infrastructure. The traditional way for the government to build a new piece of infrastructure, such as a hospital, a school, or a new road bypass, was to raise the money in taxes, or borrow it from the bond markets, and then pay builders to deliver the project. After that, the public sector would own the asset. 

The theoretical justification for Private Finance Initiatives (PFI) is that the private sector is more efficient at delivering and managing infrastructure projects than civil servants. PFI also supposedly transfers the financial risk of a construction project over-running from the public to the private sector. However earlier this year, the National Audit Office (NAO), released a new report which highlighted a lack of evidence that PFIs offer value for money for taxpayers.

The report followed the collapse of the construction and services firm Carillion which has shone a bright spotlight on the flawed process of  state contracting and outsourcing.

According to the Treasury data there are 716  PFI projects (of which 686 are operational) with a capital value of just under £60bn. Of this total the Department of Health was responsible for £13bn, the Ministry of Defence £9.5bn and the Department of Education £8.6bn.

Hammond pledged a tax crackdown with a UK “digital services tax”, aimed only at multimillion companies rather than startup businesses. On universal credit, the government attempted to neutralise the toxic issues with an extra £1bn to ‘ease issues with its rollout.’

But Hammond’s generous tax cuts to the very wealthiest households indicate that this is still very much a government for the few, not the many. 

Alison Garnham, chief executive of the Child Poverty Action Group, commented:

The work allowance increase is unequivocally good news for families receiving universal credit but a bigger salvage operation is still needed for the benefit. And bringing forward higher tax allowances – which will cost much more than the universal credit change – will mainly benefit the richest half of the population. We look forward to hearing more detail on how the secretary of state will use the extra £1bn to ease the migration of people on existing benefits to universal credit.

This is crunch time for universal credit. We hope the chancellor’s positive announcements on work allowances will be followed by a pause in the roll-out to allow for a fundamental review of its design and, crucially, for a commitment to restoring all the money that’s been taken out of universal credit.

Final comment:

 


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Wealthiest tenth of households are ‘overwhelmingly’ the biggest beneficiaries of Hammond’s budget tax cuts

Image result for Philip hammond rewards for the wealthy

The Resolution Foundation is a non-partisan think tank that works to improve the living standards of those in Britain on low to middle incomes.

The foundation’s initial comments on Hammond’s budget: 

The big print giveth and the small print taketh away.

Torsten Bell, director of the Resolution Foundation, says about the budget:

“In today’s budget, the chancellor has significantly eased – but not ended – austerity for public services. However, tough times are far from over.

The chancellor has set out plans to spend almost all of a very significant fiscal windfall on extra spending for the NHS, bringing to a close the era of falling overall public service spending. But unprotected departments are still on course for spending cuts into the 2020s – averaging 3% between 2019 and 2023.

The chancellor has also delivered a welcome boost to [‘hard working’] families on universal credit worth £630 a year.” 

Tomorrow the Resolution Foundation and the Institute for Fiscal Studies will both be publishing detailed assessments of the budget. I will be scrutinising these and commenting on them.

Jeremy Corbyn’s verdict:


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GPs told to consider making fit notes conditional on patients having appointment with work coach

Thanks to  for the copy of a patient work coach letter to GPs.

One of the most worrying comments on the above letter is that despite claiming the work coach service is voluntary, and that if a patient refuses to engage “it won’t affect any benefit they get”, the letter then goes on to suggest that doctors may consider the issuing of subsequent fit notes conditional (“with the proviso that”) on their patient attending a meeting with the work coach. That one sentence simply makes a mockery of the claim that patient engagement with work coaches is voluntary. 

Illnesses don’t respond to provisos or caveats. People don’t suddenly recover when the Department for Work and Pensions decides that they are fit for work. When job centre staff tell GPs to stop issuing sick notes to patients it can have catastrophic consequences, from which the government never seem to learn. In fact they don’t even acknowledge the terrible costs that their deeply flawed policies are inflicting on citizens. 

Julia Savage is a manager at Birkenhead Benefit Centre in Liverpool. In 2016, she wrote a letter (an ESA65B notification form) addressed to a GP regarding a seriously ill patient. It said:

We have decided your patient is capable of work from and including January 10, 2016.

“This means you do not have to give your patient more medical certificates for employment and support allowance purposes unless they appeal against this decision.

“You may need to again if their condition worsens significantly, or they have a new medical condition.” 

The GP subsequently repeatedly refused to provide him with new fit notes, even as his health deteriorated, and he died months later.

James Harrison – the patient – had been declared “fit for work” and the letter stated that he should not get further medical certificates. The Department for Work and Pensions contacted his doctor without telling him, and ordered him to cease providing sick certification, James died, aged 55.

He was very clearly not fit for work.

It is very worrying that the ESA65B form is a standardised response to GPs from the Department for Work and Pensions following an assessment where someone has been found fit for work.  

The government as boardroom doctors: political jobsworths

The Department for Work and Pensions issued a new guidance to GPs in 2013, regarding when they should issue a Fit Note. This was updated in December 2016. 

In the dogma document, doctors are warned of the dangers of “worklessness” and told they must consider “the vital role that work can play in your patient’s health”. According to the department, “the evidence is clear that patients benefit from being in some kind of regular work”

As a matter of fact, it isn’t clear at all.

The idea that people remain ill deliberately to avoid returning to work  – what Iain Duncan Smith and David Cameron termed “the sickness benefit culture” – is not only absurd, it’s very offensive. This is a government that not only disregards the professional judgements of doctors, it also disregards the judgements of ill and disabled people. However, we have learned over the last decade that political “management” of people’s medical conditions does not make people healthier or suddenly able to work.

Government policies, designed to ‘change behaviours’ of ill and disabled people have resulted in harmdistress and sometimes, in premature deaths.

Call me contrary, but whenever I am ill with my medical and not political illness, I generally trust my qualified GP or consultant to support me. I would never think of making an appointment to see the irrational likes of Esther McVey or Iain Duncan Smith for advice on lupus, or to address my health needs and treatment. 

The political de-professionalisation of medicine, medical science and specialisms (consider, for example, the ghastly implications of permitting job coaches to update patient medical files), the merging of health and employment services and the recent absurd declaration that work is a clinical “health” outcome, are all carefully calculated strategies that serve as an ideological prop and add to the justification rhetoric regarding the intentional political process of dismantling publicly funded state provision, and the subsequent stealthy privatisation of Social Security and the National Health Service. 

De-medicalising illness is also a part of that increasingly behaviourist-neoliberal process:  “Behavioural approaches try to extinguish observed illness behaviour by withdrawal of negative reinforcements such as medication, sympathetic attention, rest, and release from duties, and to encourage healthy behaviour by positive reinforcement: ‘operant-conditioning’ using strong feedback on progress.” Gordon Waddell and Kim Burton in Concepts of rehabilitation for the management of common health problems. The Corporate Medical Group, Department for Work and Pensions, UK. 

Waddell and Burton are cited frequently by the Department for Work and Pensions (DWP) as providing ‘scientific evidence’ that their policies are “verified” and “evidence based.” Yet the DWP have selectively funded their research, which unfortunately frames and constrains the theoretical starting point, research processes and the outcomes with a heavy ideological bias. 

This behaviourist framing simply shifts the focus from the medical conditions that cause illness and disability to the ‘incentives’, behaviours and perceptions of patients and ultimately, to neoliberal notions of personal responsibility and self-sufficient citizenship in the dehumanising context of a night watchman, non-welfare state, absent of any notion of human rights. 

Medication, rest, release from duties, sympathetic understanding – the remedies to illness – are being appallingly redefined as ‘perverse incentives’ for ill health, yet the symptoms necessarily precede the prescription of medication, the Orwellian renamed (and political rather than medical) “fit note” and exemption from work duties. Notions of ‘rehabilitation’ and medicine are being redefined as behaviour modification: here it is proposed that operant conditioning in the form of negative reinforcement –  punishment – will cure’ ill health. 

It’s a completely slapstick rationale, hammered into shape by a blunt instrument – political ideology. People cannot simply be ‘incentivised’ (coercion is a more appropriate term) into not being ill. Punishing people for being poor by removing their support does not ‘help’ them to stop being poor, either, despite the  doublespeak and mental gymnastic pseudoscientific rubbish the government spouts.

Turning health care into a government work programme 

The government dogmatically assert “The idea behind the fit note is that individuals do not always need to be fully recovered to go back to work, and in fact it can often help recovery to return to work.” 

It was 2015 when I wrote a breaking article about the government’s Work and Health programme, raising concerns that the Nudge Unit team were working with the Department for Work and Pensions and the Department of Health to trial social experiments aimed at finding ways of: “preventing people from falling out of the jobs market and going onto Employment and Support Allowance (ESA).” 

“These include GPs prescribing a work coach, and a health and work passport to collate employment and health information. These emerged from research with people on ESA, and are now being tested with local teams of Jobcentres, GPs and employers.”

Of course the government hadn’t announced these ‘interventions’ in the lives of ill and disabled people. I found out about it quite by chance because I happened to read Matthew Hancock’s  conference speech: The Future of Public Services.

I researched a little further and found an article in Pulse – a publication for for medical professionals – which confirmed Hancock’s comment: GP practices to provide advice on job seeking in new pilot schemeI posted my own article on the Pulse site in October 2015, raising some of my concerns.

Many of us have warned that the programme jeopardises doctor-patient confidentiality, risks alienating patients from their doctors and perverts the primary role and ethical mission of the healthcare system, which is to help people to recover from illnesses. Placing job coaches in GP surgeries makes them much less inaccessible, because it turns appointments potentially into areas of pressure and coercion. That is the very last thing someone needs when they become ill.

One worry was that the government may use the ‘intervention’ as a further opportunity for sanctioning ill and disabled people for ‘non-compliance’. People who are ill often can’t undertake work related tasks precisely because they are ill. Until recent years, this was accepted as common sense, and any expectation of sick people having to conform with such rigid welfare conditionality was quite properly regarded as both unfair and unrealistic.

I expressed concern that the introduction of  job coaches in health care settings, peddling the myth that ‘work is a health outcome’ would potentially conflict with the ethics and role of a doctor. I also stated my concern about the potential that this (then) pilot had for damaging the trust between doctors and their patients. 

In another article in 2016, titled Let’s keep the job centre out of GP surgeries and the DWP out of our confidential medical records, I outlined how GPs had raised their own concerns about sharing patient data with the Department for Work and Pensions – and quite properly so. 

Pulse reported that the Department for Work and Pensions (DWP) plans to extract information from GP records, including the number of Med3s or so-called ‘fit notes’  issued by each practice and the number of patients recorded as ‘unfit’ or ‘maybe fit’ for work, in an intrusive move described by GP leaders as amounting to “state snooping.”

Part of the reason for this renewed government attack on ill and disabled people is that the Government’s flagship fit note scheme, which replaced sick notes five years ago in the hope it would see GPs sending thousands more employees back to work to reduce sickness-related absence, despite GPs having expressed doubts since before its launch, has predicably failed.

The key reason for the failure is that employers did not take responsibility for working with employees and GPs seriously, and more than half (59%) of employers said they felt unable to support employees by making all of the legally required workplace adjustments for those who had fit notes signed as “may be fit for work.” Rather than address this issue with employers, the government has decided instead to simply coerce patients back into work without essential support.

Another reason for the failure of this scheme is that most people who need time off from work are ill and genuinely cannot return to work until they have recovered. Regardless of the government’s concern for the business and state costs of sick leave, people cannot be simply ushered out of illness and into work by the state to “contribute to the economy.”

When a GP says a person is ‘unfit for work’, they generally ARE unfit for work, regardless of whether the ‘business friendly’ government likes that or not. And regardless of the politically prescribed Orwellian renaming of sick notes, which show ‘paternalist’ linguistic behaviourism in action.

In 2017, the General Medical Council (GMC) – independent regulator for doctors in the UK – wrote a response to the government’s green paper: Improving Lives: The Work, Health and Disability Green Paper consultation. The authors of the document begin by saying ” Our purpose is to protect, promote and maintain the health and safety of the public by ensuring proper standards in the practice of medicine.”

The response continues: “Where doctors are expected to play a role in initiatives such as those set out in the Green paper, our concern is to ensure that any responsibilities that might be placed on doctors would be consistent with their professional obligations and would not risk damaging patients’ trust in their doctors. While we believe that many of the Green paper proposals are promising, we are concerned that key elements appear to present a conflict with the ethical responsibilities we place on doctors. The comments below are seeking clarification in these areas.”

And: “We understand from this Green paper, and from the Department of Work and Pensions’ published FOI response, dated 22 December 2016, that the work coaches who will conduct the mandatory health and work conversation with claimants will not be health professionals. There is a risk that claimants will not get the right support in setting health and work-related goals during this mandatory conversation if the work coach does not have clinical expertise.

“It would be helpful to know whether work coaches will be expected to have access to the claimant’s healthcare team and/or health records to inform these conversations. If so, we would appreciate reassurance that there will be a process for obtaining consent from the claimant, and providing assurance to the relevant health professionals that the individual has provided consent. Given that work coaches do not require medical expertise, we have some concerns about these conversations leading claimants to agree to health-related actions in a Health and Work ‘claimant commitment’. It seems possible that agreed actions might not be clinically appropriate for that individual or not the best course of action given their health condition. 

If a claimant commitment were reviewed by the claimant’s doctor (or other healthcare professional), and the doctor concluded that there was a health risk; then would the claimant be free to withdraw from the commitment without facing a benefits penalty? If not, then this would put the doctor and patient in a very difficult position, if it appeared that the patient had been poorly advised by the work coach and was not making an informed, voluntary decision in requesting a particular treatment or care regime from their doctor. 

We note the intention is for any agreement made in the Health and Work Conversation to be seen as voluntary. However, it seems to us that since the Conversation itself is mandatory and a Claimant commitment may influence subsequent handling of an individual’s Work Capability assessment, then in practice claimants may see these agreements as mandatory.

“As a result they may feel pressured to accept advice and make commitments which may not be appropriate in their case. This would place theirdoctors in a difficult ethical position, and we are concerned to ensure that this is not the case.

The authors add: “… we make it clear in our guidance that doctors must consider the validity of a patient’s consent to treatment if it is linked with access to benefits. Doctors should be aware that patients may be put under pressure by employers, insurers, or others to accept a particular investigation or treatment (paragraph 41, Consent: patients and doctors making decisions together).

“Difficulty could arise if a doctor does not believe that a patient is freely consenting to treatment and is instead only giving consent due to financial pressure. Doctors must be satisfied that they have valid consent before providing  treatment, which means they could be left with a difficult decision as to whether to refuse treatment in the knowledge that this could affect the patients benefit entitlements.” 

The GMC also raise concerns about how sensitive health data is collected and shared for purposes other for patients’ direct care, without patients being informed or giving consent. The government have simply proposed to access health care data to support “any assessment for financial support” and told GPs to assume consent has been given.

Promoting the myth that work is a ‘clinical outcome’ 

A Department for Work and Pensions research document published back in 2011 – Routes onto Employment and Support Allowance – said that if people believed that work was good for them, they were less likely to claim or stay on disability benefits. 

Of course it may be the case that people in better health work because they can, and have less need for healthcare services simply because they are relatively well, rather than because they work. 

From the document“The belief that work improves health also positively influenced work entry rates; as such, encouraging people in this belief may also play a role in promoting return to work.”

The aim of the research was to “examine the characteristics of ESA claimants and to explore their employment trajectories over a period of approximately 18 months in order to provide information about the flow of claimants onto and off ESA.” 

A political decision was made that people should be “encouraged” to believe that work was “good” for their health. There is no empirical basis for the belief, and the purpose of encouraging it is simply to cut the numbers of disabled people claiming Employment and Support Allowance (ESA) by “helping” them into work.

Another government document from 2014 – Psychological Wellbeing and Work – says: We know that being in work is good for wellbeing and that mental health problems are an increasing issue for the nation and so the Minister for Welfare Reform and the Minister for Care and Support jointly sought to expand the evidence base on common mental health problems.  

“A number of Government programmes assess and support those with mental health difficulties to work, but it is internationally recognised that the evidence base for successful interventions is limited. 

“The Contestable Policy Fund gives ministers alternative avenues to explore new thinking and strategies that offer cross-Government benefits. This report was commissioned through this route.” 

And: “Within the time and resources available for this study the research team did not undertake extensive assessment of the quality of the evidence base (eg assessing the research design and methodology of previous studies)”

The government have gone on to declare with authoritarian flourish that they now want to reinforce their proposal that “work is a health outcome.” Last year, a report by the Mental Health Task Force and chaired by Mind’s Paul Farmer, recommended that employment should be recognised as a ‘health outcome’.  I’m just wondering how people with, say, personality disorders, or psychosis are suddenly going to overcome the nature of their condition and all of a sudden successfully hold down a job for a minimum of six months.

Mind those large logical gaps… 

This has raised immediate concerns regarding the extent to which people will be pushed into work they are not able or ready to do, or into bad quality, low paid and inappropriate work that is harmful to them, under the misguided notion that any work will be good for them in the long run.

It has become very evident over recent years that the labour market is not delivering an adequate income for many citizens and despite “record levels of employment”, the problem seems to be getting bigger. The government’s answer to the problem has been to extend punishment those on low pay, rather than tackle employers who pay exploitative, low wages.

The idea of the state persuading doctors and other professionals to “sing from the same [political] hymn sheet”, by promoting work outcomes in social and health care settings is more than a little Orwellian. Co-opting professionals to police the welfare system is very dangerous. 

In linking receipt of welfare with health services and “state therapy,” with the single intended outcome explicitly expressed as employment, the government is purposefully conflating citizen’s widely varied needs with economic outcomes and diktats, isolating people from traditionally non-partisan networks of relatively unconditional support, such as the health service, social services, community services and mental health services.

Public services “speaking with one voice” as the government are urging, will invariably make accessing support conditional, and further isolate already marginalised social groups. Citizens’ safe spaces for genuine and objective support is shrinking as the state encroaches with strategies to micromanage those using public services. This encroachment will damage trust between people needing support and professionals who are meant to deliver essential public services, rather than simply extending government dogma, prejudices and discrimination.

State micromanagement of tenants

The GMC say in their response to the government’s proposals: “We are unclear about the evidence that might support a move to the position that ‘being in employment’ should be regarded as a ‘clinical outcome’ that healthcare professionals are expected to work towards with people of employment age seeking health-related advice and treatment. This is a highly contentious issue and indeed Dame Carol Black’s report certainly makes clear that there is limited support for this within the profession.” 

I’m not unclear. There is no evidence. In an era of small state neoliberalism and ideologically driven austerity, it is an act of sheer political expediency to claim that ‘worklessness’ is the reason for the poor health outcomes that are in fact correlated with increasing inequality, poverty and lower standards of living – higher mortality;  poorer general health, long-standing illness, limiting longstanding illness; poorer mental health, psychological distress, psychological/psychiatric morbidity; higher medical consultation, medication consumption and hospital admission rates.

Both social security and the National Health Service have been intentionally underfunded and run down by the Conservatives, who have planned and partially implemented a piecemeal privatisation process by stealth, to avoid a public backlash.

Unemployment (not ‘worklessness’ –  that’s part of the privileged discourse of neoliberalism, which serves to marginalise the structural aspects of persistent unemployment and poverty, by transforming these into individual pathologies of benefit ‘dependency ‘and ‘worklessness’) is undoubtedly associated with poverty, because welfare provision no longer meets the most basic living costs.

However to make an inferential leap and claim that work is therefore ‘good’ for health’ is incoherent, irrational and part of an elaborate political gaslighting campaign of an authoritarian government, who simply don’t want to address growing poverty and inequality caused by their own neoliberal policies.

The direction that government policy continues to be pushed in represents a serious threat to the health, welfare, wellbeing, basic human rights, democratic inclusionand lives of patients and the political independence of health professionals.


Related

The new Work and Health Programme: government plan social experiments to “nudge” sick and disabled people into work 

Illustration by Jack Hudson


My work is unfunded and I don’t make any money from it. This is a pay as you like site. If you wish you can support me by making a one-off donation or a monthly contribution. This will help me continue to research and write independent, insightful and informative articles, and to continue to support others.

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Authoritarian Brexit secretary refuses to give evidence to Parliament

Image result for Dominic Raab refuses to

The Lords European Union Committee has written to Dominic Raab MP, Secretary of State for Exiting the European Union, urging him to engage with Committees in order to facilitate scrutiny of the Withdrawal Agreement and political statement on the future UK-EU relationship.

See:

Lord Boswell, Chair of the Committee, reacted with anger to Raab’s refusal to engage and to behave in a democratically accountable manner. In a letter, he told the Brexit secretary his behaviour was ‘unacceptable.’ 

The former Conservative MP said: “Select committees have a job to do. Lack of engagement from the government, keeping us in the dark, means we can’t do that job.

He also said “Brexit was supposed to be about enhancing the role of parliament, not diminishing it – but that message doesn’t seem to have got through to ministers.”

Background

The Committee wrote the Secretary of State for Exiting the EU on 5 September 2018 inviting him to appear before the Committee as soon as possible after the October European Council, after the Secretary of State gave a Commitment in a letter of the 17 July “to give evidence on a regular basis”.

The Committee was told on Tuesday 23 October that the Secretary of State for Exiting the EU will be unable to attend or give evidence to the Committee until after a deal with the EU has been finalised. The Committee describes this as “unacceptable… [it] inhibits the Committee in fulfilling its obligations in scrutinising the progress of Brexit negotiations”.

The Committee’s letter also called on the Government to ensure that enough time is allowed between an agreement being reached and any ‘Meaningful Vote,’ so that committees can make recommendations to the two Houses. Recent reports suggest that the time allowed for committees to report on the agreement and the ‘political declaration’ on future UK-EU relations could be a little as ten days.

The letter goes on to say “…  it is imperative that both Houses—and the wider public—are able to have an informed debate. This means, among other things, that the Committees of both Houses with responsibility for scrutinising the Brexit negotiations must have an opportunity to report on the text of any agreement ahead of the ‘Meaningful Vote’—in the same way as the AFCO Committee of the European Parliament will have an opportunity to report ahead of any vote in that Parliament.

“We therefore seek your assurance that the Government will allow time for effective
Committee scrutiny of any agreement, ahead of the ‘Meaningful Vote’; and we ask you to setout your plans for engaging with Committees in order to facilitate this scrutiny.”

The Committee requested that Raab make an appearance before the end of November, saying his refusal “flies in the face of the commitment in your letter of 17 July, ‘to give evidence on a regular basis’.”

The Brexit department have been contacted for a comment. 

A little about Dominic Raab

Raab lies on the swivel eyed end of the right wing continuum. In 2017, he was branded “offensive” by then Liberal Democrat leader Tim Farron after saying “the typical user of a food bank is not someone that’s languishing in poverty, it’s someone who has a cash flow problem”. The Office For National Statistics also took issue with Raab’s claims that immigration has caused house prices to rise, demanding that he present data to back up such assertions. A document published by the Ministry of Housing, Communities and Local Government shows that the finding was based on an out-of-date model that had never been intended for this kind of analysis. 

Theresa May herself has previously spoken out against Rabb’s controversial remarks, scorning his categorization of feminists as ‘obnoxious bigots’. In an article in January 2011 on the Politics Homewebsite, Raab argued in favour of transferable paternity leave and against “the equality bandwagon” “pitting men and women against each other”. He argued in favour of a ‘consistent approach’ to sexism against men and women commenting that some feminists were “now amongst the most obnoxious bigots” and it was sexist to blame men for the recession.

He believes that the welfare state should be further reduced and his opposition to human rights and equalities is unremittingly and dangerously authoritarian. 

Raab’s opinions reflect contempt for international human rights frameworks in particular. The EU Charter of rights has not been included in the Withdrawal Bill.

Writing in the Daily Mail on prisoners votes back in 2013, Raab said: “The problem today is that the Strasbourg Court is packed with academics and politically motivated lawyers desperate to foist their ‘progressive’ agenda on the rest of Europe. The Strasbourg judges have long since given up merely interpreting the European Convention – their proper job – and are jealously usurping the power of elected lawmakers in sovereign states to create new law, inventing novel rights along the way.”

And “The Human Rights Act [UK] is bad enough. But, at least it states plainly that our courts only have to ‘take into account’ Strasbourg case-law, rather than slavishly bow to it. Yesterday, the Supreme Court shifted the goal posts, ruling that British courts must comply with Strasbourg rulings unless it involves ‘some truly fundamental principle’, or an ‘egregious oversight or misunderstanding’ of UK law.”

He also said “The wretched Human Rights Act should be replaced with a British Bill of Rights, to insulate us from the judicial onslaught from Strasbourg. And when we renegotiate the UK’s relationship with the European Union, we must shield our democracy from their ambition to impose yet another layer of European human rights law on the long-suffering British public.”

He seems to have completely missed the point of human rights. And scarily, he fails to make the connection between civil rights and democracy. 

 

Related

An introduction to Dominic Raab, the new Brexit sectarian

Government refuse to publish Brexit impact assessment. We need to ask why

The Centre for Social Justice say Brexit is ‘an opportunity’ to introduce private insurance schemes to replace contribution-based social security

European fundamental rights charter to be excluded in the EU withdrawal Bill, including protection from eugenic policy

Brexit is a zero sum neoliberal strategy


 

My work is unfunded and I don’t make any money from it. This is a pay as you like site. If you wish you can support me by making a one-off donation or a monthly contribution. This will help me continue to research and write independent, insightful and informative articles, and to continue to support others.

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